Recent Advances in Nanotechnology-Based Targeted Therapeutics for Breast Cancer Management

被引:16
作者
Alhalmi, Abdulsalam [1 ]
Beg, Sarwar [1 ,2 ]
Almalki, Waleed H. [3 ]
Alghamdi, Saad [4 ]
Kohli, Kanchan [1 ]
机构
[1] Jamia Hamdard, Sch Pharmaceut Educ & Res, Dept Pharmaceut, New Delhi 110062, India
[2] Univ Cent Lancashire, Fac Clin & Biomed Sci, Sch Pharm & Biomed Sci, Preston PR1 2HE, England
[3] Umm Al Qura Univ, Fac Med, Dept Pharmacol & Toxicol, Mecca, Saudi Arabia
[4] Umm Al Qura Univ, Fac Appl Med Sci, Lab Med Dept, Mecca, Saudi Arabia
关键词
Breast cancer; active targeted; nanocarriers; receptors; ligands; chemotherapy; LOADED POLYMERIC MICELLES; SOLID LIPID NANOPARTICLES; PEGYLATED LIPOSOMAL DOXORUBICIN; MESOPOROUS SILICA NANOPARTICLES; SERUM-ALBUMIN NANOPARTICLES; ADVANCED DRUG-DELIVERY; IN-VITRO; GROWTH-FACTOR; HYALURONIC-ACID; CO-DELIVERY;
D O I
10.2174/1389200223666220514151110
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Despite the great efforts that have been achieved in breast cancer treatment, it remains a significant cause of death in women and is a serious health problem. Treatment with chemotherapy drugs faces various challenges, such as toxicity and chemoresistance to chemotherapeutic drugs, which hinder their therapeutic success and clinical experiments. This review focuses on targeting nanocarrier approaches to target chemotherapy drugs to receptor targets that are overexpressed on the surface of breast cancer cells. In particular, the most commonly targeted nanocarriers for the chemotherapeutic agents examined by the different researcher groups, such as liposomes, dendrimers, polymeric micelles, lipid particulates, polymeric nanoparticles, and carbon nanotubes, have been reviewed. Moreover, we summarized the molecular receptors or targets that are the most commonly overexpressed in breast cancer cells and the natural and synthetic ligands studied for use as targeting moieties to functionalize chemotherapeutically loaded nanocarriers for potential specific breast cancer targeting.
引用
收藏
页码:587 / 602
页数:16
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